Current Status of Companion and Complementary Diagnostics: Strategic Considerations for Development and Launch

Clin Transl Sci. 2017 Mar;10(2):84-92. doi: 10.1111/cts.12455. Epub 2017 Feb 27.

Abstract

US Food and Drug Administration (FDA)-approved diagnostic assays play an increasingly common role in managing patients to prolong lifespan while also enhancing quality of life. Diagnostic assays can be essential for the safe and effective use of therapeutics (companion diagnostic), or may inform on improving the benefit/risk ratio without restricting drug access (complementary diagnostic). This tutorial reviews strategic considerations for drug and assay development resulting in FDA-approved companion or complementary diagnostic status.

MeSH terms

  • Biomarkers / analysis
  • Complementary Therapies / legislation & jurisprudence*
  • Diagnostic Techniques and Procedures* / economics
  • Health Services Accessibility
  • Humans
  • Insurance, Health, Reimbursement
  • Molecular Targeted Therapy / methods
  • Neoplasms / drug therapy*
  • Precision Medicine / economics
  • Precision Medicine / methods*
  • Quality of Life
  • Vereinigte Staaten
  • United States Food and Drug Administration / legislation & jurisprudence*

Substances

  • Biomarkers